Author:
Dallari Simone,Martinez Pazos Vicky,Munoz Eusse Juan,Wellens Judith,Thompson Craig,Colombel Jean-Frederic,Satsangi Jack,Cadwell Ken,Wong Serre-Yu, ,Neil Jessica Anne,Sota Stela,Jang Kyung Ku,Ching Krystal,Venzon Mericien,Yao Xiaomin,Bernard Lucie,Chen Xin,Tankelevich Michael,Navalurkar Reema,Dixon Rebekah,Helmus Drew S.,Lange Marcia Mukanga,Spiera Emily,Sangmo Lodoe
Abstract
AbstractWhile differential antibody responses SARS-CoV-2 in patients with inflammatory bowel disease (IBD) receiving infliximab and vedolizumab are well-characterized, the immune pathways underlying these differences remain unknown. Prior to COVID-19 vaccine development, we screened 235 patients with IBD receiving biological therapy for antibodies to SARS-CoV-2 and measured serum cytokines. In seropositive patients, we prospectively collected clinical data. We found a cytokine signature in patients receiving vedolizumab who are seropositive compared with seronegative for SARS-CoV-2 antibodies that may be linked to repeated SARS-CoV-2 infections. However, there were no differences between seropositive and seronegative patients receiving infliximab. In this single-center cohort of patients with IBD with anti-SARS-CoV-2 antibodies at the onset of the COVID-19 pandemic, and therefore without influence of vaccination, there is a cytokine signature in patients receiving vedolizumab but not infliximab. These findings lay the groundwork for further studies on immune consequences of viral infection in patients with IBD, which is postulated to evolve from aberrant host-microbe responses.
Funder
Leona M. and Harry B. Helmsley Charitable Trust
Publisher
Springer Science and Business Media LLC